Metal Complexes of Tridentate Beta-Ketoiminates

ABSTRACT

Metal-containing complexes of a tridentate beta-ketoiminate, one embodiment of which is represented by the structure: 
     
       
         
         
             
             
         
       
         
         
           
             wherein M is a metal such as calcium, strontium, barium, scandium, yttrium, lanthanum, titanium, zirconium, vanadium, tungsten, manganese, cobalt, iron, nickel, ruthenium, zinc, copper, palladium, platinum, iridium, rhenium, osmium; R 1  is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl, having 1 to 10 carbon atoms; R 2  is selected from the group consisting of hydrogen, alkyl, alkoxy, cycloaliphatic, and aryl; R 3  is linear or branched selected from the group consisting of alkylene, fluoroalkyl, cycloaliphatic, and aryl; R 4  is a branched alkylene bridge with at least one chiral center; R 5-6  are individually linear or branched selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, aryl, and can be connected to form a ring containing carbon, oxygen, or nitrogen atoms; n is an integer equal to the valence of the metal M.

BACKGROUND OF THE INVENTION

The semiconductor fabrication industry continues to demand novel metal source containing precursors for chemical vapor deposition processes including atomic layer deposition for fabricating conformal metal containing films on substrates such as silicon, metal nitride, metal oxide and other metal-containing layers using these metal-containing precursors.

BRIEF SUMMARY OF THE INVENTION

This invention is directed to metal containing tridentate β-ketoiminates and solutions wherein the tridentate β-ketoiminates incorporate nitrogen or oxygen functionality in the imino group. The tridentate β-ketoiminates are selected from the group represented by the structures:

wherein M is a metal having a valence of from 2 to 5. Examples of metals include calcium, magnesium, strontium, barium, scandium, yttrium, lanthanum, titanium, zirconium, vanadium, tungsten, manganese, cobalt, iron, nickel, ruthenium, zinc, copper, palladium, platinum, iridium, rhenium, and osmium. A variety of organo groups may be employed as for example wherein R¹ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl, having from 1 to 10 carbon atoms, preferably a group containing 1 to 6 carbon atoms; R² is selected from the group consisting of hydrogen, alkyl, alkoxy, cycloaliphatic, and aryl; R³ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl; R⁴ is a C₃₋₁₀ branched alkylene bridge having at least one chiral carbon atom, preferably a group containing 3 or 4 carbon atoms, thus making a five- or six-membered coordinating ring to the metal center; R⁵⁻⁶ are individually selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, aryl, and they can be connected to form a ring containing carbon, oxygen, or nitrogen atoms. The subscript n is an integer and equals the valence of the metal M.

wherein M is a metal ion selected from Group 4, 5 metals including titanium, zirconium, and hafnium; wherein R¹ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl, preferably a group containing 1 to 6 carbon atoms; R² is selected from the group consisting of hydrogen, alkyl, alkoxy, cycloaliphatic, and aryl; R³ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl; R⁴ is a C₃₋₁₀ branched alkylene bridge having at least one chiral carbon atom, preferably a group containing 3 or 4 carbon atoms, thus making a five- or six-membered coordinating ring to the metal center; R⁵⁻⁶ are individually selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, aryl, and they can be connected to form a ring containing carbon, oxygen, or nitrogen atoms; R⁷ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl; wherein m and n are at least 1 and the sum of m+n is equal to the valence of the metal.

Several advantages can be achieved through these metal-containing tridentate β-ketoiminates as precursors for chemical vapor deposition or atomic layer deposition, and these include:

-   -   an ability to form reactive complexes in good yield;     -   an ability to form monomeric complexes, particularly calcium and         strontium complexes, coordinated with one kind of ligand, thus         allowing one to achieve a high vapor pressure;     -   an ability to significantly increase the thermal stability of         resulting metal complexes via introduction of branched alkylene         bridge having at least one chiral carbon atom between the two         nitrogen atoms compared to those without chiral centers between         the two nitrogen atoms     -   an ability to produce highly conformal metal thin films suited         for use in a wide variety of electrical applications;     -   an ability to form highly conformal metal oxide thin films         suited for use in microelectronic devices;     -   an ability to enhance the surface reaction between the         metal-containing tridentate β-ketoiminates and the surface of a         substrate due to the high chemical reactivity of the complexes.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a drawing representative of the crystal structure of bis(2,2-dimethyl-5-(1-dimethylamino-2-propylimino)-3-hexanonato-N,O,N′)strontium.

FIG. 2 is thermogravimetric analysis (TGA) diagrams of bis(2,2-dimethyl-5-(1-dimethylamino-2-propylimino)-3-hexanonato-N,O,N′)strontium (solid line) vs bis(2,2-dimethyl-5-(dimethylaminoethyl-imino)-3-hexanonato-N,O,N′)strontium (dashed line), indicating the new Sr complex with a chiral center (solid line) is much more stable than that without chiral center between the two nitrogen atoms (dashed line), thus leaving almost no residue.

FIG. 3 is a drawing representing the crystal structure of bis(2,2-dimethyl-5-(1-dimethylamino-2-propylimino)-3-hexanonato-N,O,N′)nickel.

FIG. 4 is thermogravimetric analysis (TGA) diagrams of bis(2,2-dimethyl-5-(1-dimethylamino-2-propylimino)-3-hexanonato-N,O,N′)nickel (solid line) vs bis(2,2-dimethyl-5-(dimethylaminoethyl-imino)-3-hexanonato-N,O,N′)nickel (dashed line), indicating the new Ni complex with a chiral center (solid line) is much more stable than that without chiral center between the two nitrogen atoms (dashed line), thus leaving less than 2% residue.

FIG. 5 is comparison of vapor pressure of bis(2,2-dimethyl-5-(1-dimethylamino-2-propylimino)-3-hexanonato-N,O,N′)strontium (solid line) vs bis(2,2-dimethyl-5-(dimethylaminoethyl-imino)-3-hexanonato-N,O,N′)strontium (dashed line), indicating the new Sr complex with a chiral center (solid line) is more volatile than that without chiral center between the two nitrogen atoms (dashed line) although the molecular weight of bis(2,2-dimethyl-5-(dimethylaminoethyl-imino)-3-hexanonato-N,O,N′)strontium is smaller than bis(2,2-dimethyl-5-(1-dimethylamino-2-propylimino)-3-hexanonato-N,O,N′)strontium.

DETAILED DESCRIPTION OF THE INVENTION

This invention is related to metal-containing tridentate β-ketoiminate precursors and their solutions which are useful for fabricating conformal metal containing films on substrates such as silicon, metal nitride, metal oxide and other metal layers via deposition processes, e.g., CVD and ALD. Such conformal metal containing films have applications ranging from computer chips, optical device, magnetic information storage, to metallic catalyst coated on a supporting material. In contrast to prior tridentate β-ketoiminate precursors, the tridentate β-ketoiminate ligands incorporate at least one amino organo imino functionality which is in contrast to the literatures reported alkoxy group as the donating ligand, most importantly they contain a branched alkylene bridge having at least one chiral carbon atom between the two nitrogen atoms.

Oxidizing agents for vapor deposition process include oxygen, hydrogen peroxide and ozone and reducing agents for deposition processes include hydrogen, hydrazine, monoalkylhydrazine, dialkylhydrazine, and ammonia.

One type of structure in the metal precursor is illustrated in structure 1A below where the metal M has a valence of 2 having the formula:

wherein M is selected from group 2, 8, 9, 10 metal atoms. In this precursor it is preferred that R¹ is a C₁₋₆ alkyl group, preferably a t-butyl or t-pentyl group when the metal is strontium and barium and C₁₋₆ when cobalt or nickel, R² and R³ are methyl groups, R⁵ and R⁶ are individually lower C₁₋₃, preferably methyl groups and R⁴ is a C₃₋₁₀ branched alkylene bridge having at least one chiral carbon atom, preferably a group containing 3 or 4 carbon atoms. Preferred metals are calcium, strontium, barium, iron, cobalt, and nickel.

Another type of structure within the first class of metal complexes containing tridentate β-ketoiminate ligands is illustrated in structure 2A below where the metal M has a valence of 3 having the formula:

wherein M is selected from group 3 metal atoms. In this precursor it is preferred that R¹ is a C₄₋₆ alkyl group, preferably a t-butyl and t-pentyl group, R² and R³ are methyl groups, R⁵ and R⁶ are individually lower C₁₋₃ alkyl, preferably methyl groups, and R⁴ is a C₃₋₁₀ branched alkylene bridge having at least one chiral carbon atom, preferably a group containing 3 or 4 carbon atoms. Preferred metals are scandium, yttrium, and lanthanum.

The second class of metal-containing precursors are comprised of tridentate β-ketoiminate ligands as shown in formula B:

wherein M is a Group 4 or 5 metal such as titanium, zirconium, or hafnium. As shown the complex consists of at least one alkoxy ligand and a tridentate β-ketoiminato ligand having at least one amino organo imino functionality. The preferred R¹⁻⁶ groups are the same as in formula A. The preferred R⁷ group is a linear or branched alkyl, e.g., iso-propyl, butyl, sec-butyl, and tert-butyl, m and n are at least 1 and the sum of m+n is equal to the valence of the metal

The tridentateβ-ketoiminate ligands can be prepared by well known procedure such as the Claisen condensation of a bulky ketone and an ethyl ester in presence of a strong base such as sodium amide or hydride, followed by another known procedure such as Schiff base condensation reaction with alkylaminoalkylamine. The ligands can be purified via vacuum distillation for a liquid or crystallization for solid.

As a preferred method for the formation of high yield and thermal stable tridentate ligands, it is preferred to choose a bulky R¹ group, e.g., C₄₋₆ alkyl groups without hydrogen attached to the carbon connected to the ketone functionality, most preferred R¹ group is tert-butyl or tert-pentyl. The R¹ group prevents side reactions occurring in the following Schiff condensation and later protecting the metal centers from inter-molecular interaction. There is a competing issue and that is that the R¹⁻⁷ groups in the tridentate ligands should be as small as possible in order to decrease the molecular weight of the resulting metal-containing complexes and allow the achievement of complexes having a high vapor pressure. The preferred R⁴ is a branched alkylene bridge having at least one chiral carbon atom, most preferably a group containing 3 or 4 carbon atoms in order to make the resulting complexes more stable via forming a five- or six-membered coordinating ring to the metal center. The chiral center in the ligand plays a crucible in terms of lowering down the melting point as well as increasing the thermal stability.

The metal-containing complexes can then be prepared via the reaction of the resulting tridentate ligands with pure metal, metal amide, metal hydride, and metal alkoxide. The metal-containing complexes can also be prepared via reacting the tridentate ligand with alkyl lithium or potassium hydride to provide the lithium or potassium salt of the ligand, then followed by reaction with metal halide, MX_(n) (X═Cl, Br, I; n=2, 3). The group 4 and 5 mixed ligand complexes can be made via changing the ratio of metal alkoxide to the tridentate ligands.

These metal-containing complexes with tridentateβ-ketoiminate ligands can be employed as potential precursors to make thin metal or metal oxide films via either the chemical vapor deposition (CVD) or atomic layer deposition (ALD) method at temperatures less than 500° C. The CVD process can be carried out with or without reducing or oxidizing agents whereas an ALD process usually involves the employment of another reactant such as a reducing agent or oxidizing agent.

For multi-component metal oxide, these complexes can be premixed if they have the same tridentate β-ketoiminate ligands. These metal-containing complexes with tridentate β-ketoiminate ligands can be delivered in vapor phase into a CVD or ALD reactor via well-known bubbling or vapor draw techniques. A direct liquid delivery method can also be employed by dissolving the complexes in a suitable solvent or a solvent mixture to prepare a solution with a molar concentration from 0.001 to 2 M depending the solvent or mixed-solvents employed.

The solvent employed in solubilizing the precursor for use in a deposition process may comprise any compatible solvent or their mixture including aliphatic hydrocarbons, aromatic hydrocarbons, ethers, esters, nitrites, and alcohols. The solvent component of the solution preferably comprises a solvent selected from the group consisting of glyme solvents having from 1 to 20 ethoxy —(C₂H₄O)— repeat units; C₂-C₁₂ alkanols, organic ethers selected from the group consisting of dialkyl ethers comprising C₁-C₆ alkyl moieties, C₄-C₈ cyclic ethers; C₁₂-C₆₀ crown O₄-O₂₀ ethers wherein the prefixed C_(i) range is the number i of carbon atoms in the ether compound and the suffixed O_(i) range is the number i of oxygen atoms in the ether compound; C₆-C₁₂ aliphatic hydrocarbons; C₆-C₁₈ aromatic hydrocarbons; organic esters; organic amines, polyamines and organic amides.

Another class of solvents that offers advantages is the organic amide class of the form RCONR′R″ wherein R and R′ are alkyl having from 1-10 carbon atoms and they can be connected to form a cyclic group (CH₂)_(n), wherein n is from 4-6, preferably 5, and R″ is selected from alkyl having from 1 to 4 carbon atoms and cycloalkyl. N-methyl- or N-ethyl- or N-cyclohexyl-2-pyrrolidinones, N,N-Diethylacetamide, and N,N-Diethylformamide are examples.

The following example illustrates the preparation of the metal-containing complexes with tridentate β-ketoiminate ligands as well as their use as precursors in metal-containing film deposition processes.

EXAMPLE 1 Synthesis of 2,2-dimethyl-5-(1-dimethylamino-2-propylimino)-3-hexanone

To a solution of 13.55 g (95.29 mmol) 2,2-dimethyl-3,5-hexanedione in 150 mL of THF containing with 20 g (140.81 mmol) of sodium sulfate was added 11.68 g (114.34 mmol) of 1-dimethylamino-2-propylamine. Reaction mixture was heated to 65° C. for 72 hours. After completion, THF was evaporated under vacuum and excess 1-dimethylamino-2-propylamine was distilled by heating the mixture at 80° C. under 140 mTorr vacuum for one hour. Residual oil was subjected to vacuum transfer heating at 110° C. under 100 mTorr vacuum. 18.75 g of a lime-green yellow oil was obtained and GC analysis indicates 99% purity. The yield was 87%.

¹H NMR (500 MHz, C₆D₆): δ=11.51 (s, 1H), 5.20 (s, 1H), 3.24 (m, 1H), 1.91 (m, 2H), 1.91 (s, 6H), 1.60 (s, 3H), 1.32 (s, 9H), 0.94 (d, 3H).

EXAMPLE 2 Synthesis of bis(2,2-dimethyl-5-(1-dimethylamino-2-propylimino)-3-hexanonato-N,O,N′)strontium

To a solution of 1 g (1.81 mmol) Sr(N(SiMe₃)₂)₂.(THF)₂ in 10 mL THF was added 0.82 g (3.62 mmol) 2,2-dimethyl-5-(1-dimethylamino-2-propylimino)-3-hexanone in 10 mL of THF dropwise at room temperature. Stirred for 16 hours. THF was evaporated off under vacuum to provide an off-white solid that was taken up as a solution in hexanes. Evaporated off hexanes and dry solid was recrystallized in pentane at room temperature. 0.48 g of clear needle-like crystals were obtained (50% yield based on Sr).

Elemental analysis: calculated for C26H50N4O2Sr: C, 58.01; N, 10.40; H, 9.36. Found: C, 56.07; N, 10.10; H, 8.86. ¹H NMR (500 MHz, C₆D₆): δ=5.12 (s, 1H), 3.42 (m, 1H), 3.32 (t, 1H), 1.96 (b, 2H), 1.83 (s, 6H), 1.72 (b, 2H), 1.41 (s, 9H), 0.94 (d, 3H).

A colorless crystal was structurally characterized by single crystal analysis. The structure shows strontium coordinated with two oxygen and four nitrogen atoms from the two tridentate ketominate ligands in a distorted octahedral environment. This is illustrated in FIG. 1 in which there are ethylene bridges between the two nitrogen atoms of the imino functionality for R⁴ shown as C4, C5 and C18, C17. C4 and C17 are chiral atoms as they are connected to four different substituents, i.e. H, N1, C11, C5 for C4 and H, N3, C18, C24 for C17.

FIG. 2 shows a TGA of the compound of Example 2 having ethylene bridges with chiral centers between the two nitrogen atoms of the imino functionality for R⁴; in contrast to the analogous compound where R⁴ is an ethylene bridge without chiral centers. The compound of Example 2 is shown by the solid line, while the analogous compound where R⁴ is an ethylene bridge is shown by the dotted line. A larger residue in a TGA analysis typifies compounds having less stability. Thus, the compound of Example 2 has less than 1% residue whereas the analogous compound without chiral centers over 14% residue, indicating a substantial enhancement in thermal stability necessary when used as a precursor to deposit metal-containing films in a deposition in semiconductor fabrication.

EXAMPLE 3 Synthesis of bis(2,2-dimethyl-5-(1-dimethylamino-2-propylimino)-3-hexanonato-N,O,N′)nickel

To a solution of 3.49 g (15.43 mmol) 2,2-dimethyl-5-(1-dimethylamino-2-propylimino)-3-hexanone in 10 mL of hexanes at −78° C. in dry ice/acetone bath was added 6.17 mL (15.43 mmol) of 2.5M n-butyl lithium in hexanes dropwise. Warmed solution to room temperature and left to stir for one hour. Hexanes was evaporated from solution under vacuum and a residual sticky yellow oil was obtained. 20 mL of THF was added to the residual and this solution was added to 1.00 g (7.72 mmol) NiCl₂ in 10 mL of THF at room temperature. Stirred for 96 hours under argon heating at 60° C. Evaporated off THF under vacuum and residual dark green solid was taken up in hexanes, heated, and filtered. Evaporated hexanes under vacuum and obtained 3.5 g of a sticky dark green solid that was sublimed at 100° C. under 65 mTorr of vacuum for 48 hours yielding 2.8 g of a green solid (70% yield). Sublimed material was recrystallized by slow evaporation of pentane at room temperature.

Elemental Analysis: calculated for C26H50N4NiO2: C, 61.30; H, 9.89; N, 11.00. Found: C, 59.18; H, 9.09; N, 10.84.

A dark green crystal was structurally characterized by single crystal analysis. The structure shows nickel coordinated with two oxygen and four nitrogen atoms from the two tridentate ketominate ligands in a distorted octahedral environment. This is illustrated in FIG. 3 in which there are ethylene bridges between the two nitrogen atoms of the imino functionality for R⁴ shown as C9, C11 and C22, C23. C9 and C22 are chiral atoms as they are connected to four different substituents, i.e. H, N1, C10, C11 for C9 and H, N3, C23, C24 for C22.

FIG. 4 shows a TGA of the compound of Example 3 having ethylene bridges with chiral centers between the two nitrogen atoms of the imino functionality for R⁴; in contrast to the analogous compound where R⁴ is an ethylene bridge without chiral centers. The compound of Example 3 is shown by the solid line, while the analogous compound where R⁴ is an ethylene bridge without chiral centers is shown by the dotted line. A larger residue in a TGA analysis typifies compounds having less stability. Thus, the compound of Example 3 has approximately less than 3% residue whereas the analogous compound over 13% residue, indicating a substantial enhancement in thermal stability necessary when used as a precursor to deposit metal-containing films in a deposition in semiconductor fabrication.

EXAMPLE 4 Synthesis of Ti(O-^(i)Pr)₃(2,2-dimethyl-5-(1-dimethylamino-2-propylimino)-3-hexanonato

To a solution of 1 g (3.52 mmol) titanium(IV)isopropoxide in 15 mL of hexanes was added 0.80 g (3.52 mmol) 2,2-dimethyl-5-(1-dimethylamino-2-propylimino)-3-hexanone and reaction mixture was heated to 60° C. for 16 hours. Evaporated off volatiles under vacuum and obtained 1.59 g of a crude grainy oil.

¹H NMR (500 MHz, C₆D₆): δ=5.32 (s, 1H), 5.10 (b, 3H), 3.20 (m, 1H), 2.40 (b, 2H), 2.40 (b, 6H), 1.64 (s, 3H), 1.39 (d, 18H), 1.36 (s, 9H), 1.27 (b, 3H).

One of the crucial requirements for precursors employed for chemical vapor deposition and atomic layer deposition is that the precursor has to be stable during the delivery temperature, generally ranging from 40 to 150° C. The thermogravimetric analysis (TGA) is widely used as a tool to screen compounds. The measurements of the compounds of the present invention were carried out in open aluminum crucibles with sample sizes of 10 to 20 mg inside a dry box. The temperature ramp rate is usually 10 C.°/min. As the temperature increases, the compound starts to undergo either vaporization or decomposition or both. Pure vaporization leads to almost no residue, whereas vaporization plus decomposition results in certain degree of residue. Generally speaking, less residue in a TGA diagram suggests the compound is more thermally stable, thus more suitable to be a precursor for fabricating thin films. As shown in FIGS. 2 and 4, the compounds revealed in this invention have much less than residues than those prior analogues, suggesting they are more thermally stable and have a better capability to be employed as precursors. On the other hand, introduction of chiral centers is one approach to increase the thermal stability, as well as to lower the melting point of resulting metal compounds. A molecule is chiral if it cannot be superimposed on its mirror image, the two mirror images of such a molecule are referred to as enantiomers. If a carbon atom has four different substituents connected to it, it is chiral. For compounds in Example 2 and 3, there are two chiral carbon atoms, implying there are three enantiomers co-existing in the solid state, which scramble around, weakening the intermolecular interaction, thus increasing the volatility, as shown in FIG. 5, although bis(2,2-dimethyl-5-(dimethylaminoethyl-imino)-3-hexanonato-N,O,N′)strontium is smaller than bis(2,2-dimethyl-5-(1-dimethylamino-2-propylimino)-3-hexanonato-N,O,N′)strontium, and, in theory, bis(2,2-dimethyl-5-(1-dimethylamino-2-propylimino)-3-hexanonato-N,O,N′)strontium should be less volatile than bis(2,2-dimethyl-5-(dimethylaminoethyl-imino)-3-hexanonato-N,O,N′)strontium. 

1. A metal containing complex represented by the structures selected from the group consisting of:

wherein M is a metal group having a valence of from 2 to 5 wherein R¹ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl, having from 1 to 10 carbon atoms; R² is selected from the group consisting of hydrogen, alkyl, alkoxy, cycloaliphatic, and aryl; R³ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl; R⁴ is a C₃₋₁₀ branched alkylene bridge having at least one chiral carbon atom; R⁵⁻⁶ are individually selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, aryl, and heterocyclic containing either oxygen, or nitrogen atoms; n is an integer equal to the valence of the metal M;

wherein M is a metal ion selected from Group 4 and 5 metals; wherein R¹ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl, having from 1 to 10 carbon atoms; R² is selected from the group consisting of hydrogen, alkyl, alkoxy, cycloaliphatic, and aryl; R³ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl; R⁴ is a C₃₋₁₀ branched alkylene bridge having at least one chiral carbon atom; R⁵⁻⁶ are individually selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, aryl, or heterocyclic containing an oxygen, or nitrogen atom; R⁷ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl; and wherein m and n are at least 1 and the sum of m plus n is equal to the valence of the metal M.
 2. The metal containing complex of claim 1 structure A wherein M is selected from the group consisting of calcium, strontium, barium, scandium, yttrium, lanthanum, titanium, zirconium, vanadium, tungsten, manganese, cobalt, iron, nickel, ruthenium, zinc, copper, palladium, platinum, iridium, rhenium, and osmium.
 3. The metal containing complex of claim 2 wherein R¹ is selected from the group from t-butyl and t-pentyl, R² and R³ are individually selected from the group consisting of methyl and ethyl, R⁴ is a C₃ alkylene bridge with a chiral center, and R⁵ and R⁶ are individually selected from the group consisting of methyl and ethyl.
 4. The metal containing complex of claim 3 wherein M is strontium, R¹ is t-butyl, R² and R³ are methyl, R⁴ is a C₃ alkylene bridge with a chiral center and R⁵ and R⁶ are selected from the group consisting of methyl and ethyl.
 5. The metal containing complex of claim 1 represented by the structure B: wherein M is selected from the group consisting of titanium, zirconium, hafnium, vanadium, niobium, and tantalum.
 6. The metal containing complex of claim 5 wherein R¹ is selected from the group consisting of C₁₋₅ alkyl, R² and R³ are individually selected from the group consisting of methyl and ethyl, R⁴ is a C₃₋₄ alkylene bridge with at least one chiral centers, R⁵ and R⁶ are individually selected from the group consisting of methyl and ethyl, and R⁷ is selected the group consisting of methyl, ethyl, propyl, iso-propyl, n-butyl, sec-butyl, and tert-butyl.
 7. The metal containing complex of claim 5 wherein M is Ti, R¹ is methyl, R² and R³ are methyl, R⁴ is a C₃ alkylene bridge with one chiral center and R⁵ and R⁶ are methyl.
 8. The metal containing complex of claim 5 wherein M is Hf, R¹ is methyl, R² and R³ are methyl, R⁴ is a C₃ alkylene bridge with one chiral center and R⁵ and R⁶ are methyl.
 9. The metal containing complex of claim 5 wherein M is Zr, R¹ is methyl, R² and R³ are methyl, R⁴ is a C₃ alkylene bridge with one chiral center and R⁵ and R⁶ are methyl.
 10. The metal containing complex of claim 5 wherein M is Ti, R¹ is t-butyl, R² and R³ are methyl, R⁴ is a C₃ alkylene bridge and R⁵ and R⁶ are methyl.
 11. The metal containing complex of claim 5 wherein M is Hf, R¹ is t-butyl, R² and R³ are methyl, R⁴ is a C₃ alkylene bridge with one chiral center and R⁵ and R⁶ are methyl.
 12. The metal containing complex of claim 5 wherein M is Zr, R¹ is t-butyl, R² and R³ are methyl, R⁴ is a C₃ alkylene bridge with one chiral center and R⁵ and R⁶ are methyl.
 13. The metal containing complex of claim 1 dissolved in a solvent selected from the group consisting of glyme solvents having from 1 to 20 ethoxy —(C₂H₄O)— repeat units; C₂-C₁₂ alkanols, organic ethers selected from the group consisting of dialkyl ethers comprising C₁-C₆ alkyl moieties, C₄-C₈ cyclic ethers; C₁₂-C₆₀ crown O₄-O₂₀ ethers wherein the prefixed C_(i) range is the number i of carbon atoms in the ether compound and the suffixed O_(i) range is the number i of oxygen atoms in the ether compound; C₆-C₁₂ aliphatic hydrocarbons; C₆-C₁₈ aromatic hydrocarbons; organic esters; organic amines; and polyamines and organic amides.
 14. The metal containing complex of claim 13 wherein the solvent is an organic amide selected from the group consisting N-methyl-2-pyrrolidinone, N-ethyl-2-pyrrolidinone, N-cyclohexyl-2-pyrrolidinone, N,N-Diethylacetamide, and N,N-Diethylformamide.
 15. A vapor deposition process for forming a conformal metal oxide thin film on a substrate wherein a precursor source and an oxygen containing agent are introduced to a deposition chamber and a metal oxide film deposited on a substrate, the improvement which comprises using as said precursor source a metal containing complex represented by the structures selected from the group consisting of:

wherein M is a metal group having a valence of from 2 to 5 wherein R¹ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl, having from 1 to 10 carbon atoms; R² is selected from the group consisting of hydrogen, alkyl, alkoxy, cycloaliphatic, and aryl; R³ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl; R⁴ is a C₃₋₁₀ branched alkylene bridge having at least one chiral carbon atom; R⁵⁻⁶ are individually selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, aryl, and heterocyclic containing either oxygen, or nitrogen atoms; n is an integer equal to the valence of the metal M;

wherein M is a metal ion selected from Group 4 and 5 metals; wherein R¹ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl, having from 1 to 10 carbon atoms; R² is selected from the group consisting of hydrogen, alkyl, alkoxy, cycloaliphatic, and aryl; R³ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl; R⁴ is a C₃₋₁₀ branched alkylene bridge having at least one chiral carbon atom; R⁵⁻⁶ are individually selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, aryl, or heterocyclic containing an oxygen, or nitrogen atom; R⁷ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl; and wherein m and n are at least 1 and the sum of m plus n is equal to the valence of the metal M.
 16. The vapor deposition process of claim 15 wherein the vapor deposition process is selected from the group consisting of chemical vapor deposition, plasma enhanced chemical vapor deposition, atomic layer deposition, and plasma enhanced atomic layer deposition.
 17. The vapor deposition process of claim 15 wherein the oxygen containing agent is selected from the group consisting of water, O₂, H₂O₂, ozone and mixtures thereof.
 18. A vapor deposition process for forming a conformal metal thin film on a substrate wherein a precursor source and a reducing agent are introduced to a deposition chamber and a metal film deposited on a substrate, the improvement which comprises using as said precursor source a metal containing complex represented by the structures selected from the group consisting of:

wherein M is a metal group having a valence of from 2 to 5 wherein R¹ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl, having from 1 to 10 carbon atoms; R² is selected from the group consisting of hydrogen, alkyl, alkoxy, cycloaliphatic, and aryl; R³ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl; R⁴ is a C₃₋₁₀ branched alkylene bridge having at least one chiral carbon atom; R⁵⁻⁶ are individually selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, aryl, and heterocyclic containing either oxygen, or nitrogen atoms; n is an integer equal to the valence of the metal M;

wherein M is a metal ion selected from Group 4 and 5 metals; wherein R¹ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl, having from 1 to 10 carbon atoms; R² is selected from the group consisting of hydrogen, alkyl, alkoxy, cycloaliphatic, and aryl; R³ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl; R⁴ is a C₃₋₁₀ branched alkylene bridge having at least one chiral carbon atom; R⁵⁻⁶ are individually selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, aryl, or heterocyclic containing an oxygen, or nitrogen atom; R⁷ is selected from the group consisting of alkyl, fluoroalkyl, cycloaliphatic, and aryl; and wherein m and n are at least 1 and the sum of m plus n is equal to the valence of the metal M.
 19. The vapor deposition process of claim 18 wherein the reducing agent is selected from the group consisting of hydrogen, hydrazine, monoalkylhydrazine, dialkylhydrazine, ammonia, and mixtures thereof.
 20. A vapor deposition process for forming a conformal metal oxide thin film on a substrate wherein a solution of precursor source and an oxygen containing agent are introduced to a deposition chamber and a metal oxide film deposited on a substrate, the improvement which comprises using a solution of comprised of the metal containing complex of claim 15 dissolved in a solvent selected from the group consisting of glyme solvents having from 1 to 20 ethoxy —(C₂H₄O)— repeat units; C₂-C₁₂ alkanols, organic ethers selected from the group consisting of dialkyl ethers comprising C₁-C₆ alkyl moieties, C₄-C₈ cyclic ethers; C₁₂-C₆₀ crown O₄-O₂₀ ethers wherein the prefixed C_(i) range is the number i of carbon atoms in the ether compound and the suffixed O_(i) range is the number i of oxygen atoms in the ether compound; C₆-C₁₂ aliphatic hydrocarbons; C₆-C₁₈ aromatic hydrocarbons; organic esters; organic amines; and polyamines and organic amides.
 21. A vapor deposition process for forming a conformal metal thin film on a substrate wherein a solution of a precursor source and a reducing agent are introduced to a deposition chamber and a metal film deposited on a substrate, the improvement which comprises using a solution comprised of the metal containing complex of claim 18 dissolved in a solvent selected from the group consisting of glyme solvents having from 1 to 20 ethoxy —(C₂H₄O)— repeat units; C₂-C₁₂ alkanols, organic ethers selected from the group consisting of dialkyl ethers comprising C₁-C₆ alkyl moieties, C₄-C₈ cyclic ethers; C₁₂-C₆₀ crown O₄-O₂₀ ethers wherein the prefixed C_(i) range is the number i of carbon atoms in the ether compound and the suffixed O_(i) range is the number i of oxygen atoms in the ether compound; C₆-C₁₂ aliphatic hydrocarbons; C₆-C₁₈ aromatic hydrocarbons; organic esters; organic amines; and polyamines and organic amides. 